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Clinical Project Manager Site Activation Jobs (NOW HIRING)

Emerus

Clinical Project Manager

Develop and manage Activation and Operations Readiness plans for new hospital openings * Lead end ... Travel to all hospital locations as required; be on-site at hospitals at pivotal times during ...

Emerus

Clinical Project Manager

Develop and manage Activation and Operations Readiness plans for new hospital openings * Lead end ... Travel to all hospital locations as required; be on-site at hospitals at pivotal times during ...

Pharmaron

Clinical Project Manager

Baltimore, MD

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... Partner with Business Development to support feasibility assessments and site qualification ...

Pharmaron

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... Partner with Business Development to support feasibility assessments and site qualification ...

Pharmaron

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

The Clinical Project Manager (CPM) is the single, accountable leader for early-phase (FIH, SAD/MAD ... Partner with Business Development to support feasibility assessments and site qualification ...

PharmaOut

Clinical Project Manager

Gaithersburg, MD · On-site

... Site Head. Location: Gaithersburg, Maryland Responsibilities: Participates in the planning ... Provides updates on project status and deliverables to Clinical Project Management leads ...

Terumo

Job Summary Clinical Project Manager (CPM) is key to the success of the overall conduct of a ... Provide centralized site support, communication and coordination to assure timely completion of ...

New

Alnylam Pharmaceuticals

Sr. Manager, Study Start Up

... and site activation activities in Phase I-III and real-world evidence clinical trials. This team ... The Senior Manager, Study Start-up creates project plans for efficient implementation and oversight ...

PSI CRO

Clinical Project Manager

... Site Management Associates (SMAs) * Participating in feasibility research * Supporting business ... Regional clinical project management experience, including management of all project services from ...

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How much do clinical project manager site activation jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical project manager site activation in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

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For Clinical Project Manager Site Activation jobs, the most frequently searched job titles are:

Infographic showing various Clinical Project Manager Site Activation job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) - UK Remote

Remote

MCRA, LLC
Medical Equipment and Supplies Manufacturing • 51 - 200 employees
Learn more about MCRA, LLCexternal

Other

Posted 4 days ago

Job description

Job Title: Freelance Site Activation Specialist

We are seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial start-up and site activation activities.

The primary focus of this role will be UK submission document collection and preparation, site document review, Informed Consent Form (ICF) adaptations, and regulatory submission support. The successful candidate will work closely with investigative sites and internal study teams to ensure submission packages are complete, compliant, and delivered according to project timelines.

Key Responsibilities
  • Collect, review, and prepare site and regulatory documentation required for UK clinical trial submissions
  • Support the preparation and submission of regulatory packages in accordance with study requirements and local regulations
  • Perform and coordinate Informed Consent Form (ICF) adaptations and associated document updates
  • Review essential site documentation to support Regulatory Green Light readiness
  • Liaise directly with investigative sites to obtain, track, and resolve outstanding documentation
  • Ensure the completeness, accuracy, and quality of submission packages
  • Maintain study tracking systems, timelines, and submission records
  • Support site activation activities and monitor progress against project milestones
  • Collaborate closely with Site Activation Managers, Regulatory Affairs, Project Management, and other cross-functional teams
  • Ensure compliance with ICH-GCP, local UK regulations, and study-specific requirements
Requirements
  • Based in the United Kingdom
  • Minimum 2–3 years of experience in Site Activation, Study Start-Up, Regulatory Affairs, or Clinical Research
  • Strong experience with site document collection, review, and submission preparation
  • Experience supporting clinical trial regulatory submissions in the UK
  • Experience performing ICF adaptations
  • Solid understanding of site activation and study start-up processes
  • Strong attention to detail and ability to manage multiple priorities and timelines
  • Bachelor's degree in Life Sciences or a related field
  • Fluent English communication skills, both written and verbal

Apply